230 related articles for article (PubMed ID: 7878622)
21. Analysis of platelet glycoproteins in thrombocytopathias using the lectin-avidin-biotin-peroxidase (LABP) technique.
Kehrel B; Kokott R; Stenzinger W; Balleisen L
Folia Haematol Int Mag Klin Morphol Blutforsch; 1988; 115(4):425-9. PubMed ID: 2465945
[TBL] [Abstract][Full Text] [Related]
22. Use of the electron microscope for diagnosis of platelet disorders.
White JG
Semin Thromb Hemost; 1998; 24(2):163-8. PubMed ID: 9579638
[TBL] [Abstract][Full Text] [Related]
23. Inherited platelet disorders and oral health.
Valera MC; Kemoun P; Cousty S; Sie P; Payrastre B
J Oral Pathol Med; 2013 Feb; 42(2):115-24. PubMed ID: 22583386
[TBL] [Abstract][Full Text] [Related]
24. A point mutation in glycoprotein IX coding sequence (Cys73 (TGT) to Tyr(TAT)) causes impaired surface expression of GPIb/IX/V complex in two families with Bernard-Soulier syndrome.
Noda M; Fujimura K; Takafuta T; Shimomura T; Fujii T; Katsutani S; Fujimoto T; Kuramoto A; Yamazaki T; Mochizuki T; Matsuzaki M; Sano M
Thromb Haemost; 1996 Dec; 76(6):874-8. PubMed ID: 8972003
[TBL] [Abstract][Full Text] [Related]
25. Congenital disorders associated with platelet dysfunctions.
Nurden P; Nurden AT
Thromb Haemost; 2008 Feb; 99(2):253-63. PubMed ID: 18278172
[TBL] [Abstract][Full Text] [Related]
26. Biochemical and molecular basis of Bernard-Soulier syndrome: a review.
de la Salle C; Lanza F; Cazenave JP
Nouv Rev Fr Hematol (1978); 1995; 37(4):215-22. PubMed ID: 8904201
[TBL] [Abstract][Full Text] [Related]
27. Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function.
Ghosh K; Nair S; Kulkarni B; Khare A; Shetty S; Mohanty D
Platelets; 2003 Sep; 14(6):351-4. PubMed ID: 14602548
[TBL] [Abstract][Full Text] [Related]
28. Mutations in the beta3 gene giving rise to type I Glanzmann thrombasthenia in two families in Portugal.
Garcia LC; Breillat C; Lima M; Combrié R; Morais S; Teixera Mdos A; Campos M; Justica B; Nurden AT
Platelets; 2004 Feb; 15(1):15-22. PubMed ID: 14985172
[TBL] [Abstract][Full Text] [Related]
29. First Turkish case of Bernard-Soulier syndrome associated with GPIX N45S.
Dağistan N; Kunishima S
Acta Haematol; 2007; 118(3):146-8. PubMed ID: 17804902
[TBL] [Abstract][Full Text] [Related]
30. [Platelet membrane glycoproteins and the molecular mechanisms of hereditary platelet dysfunction].
Moroi M; Jung SM
Nihon Rinsho; 1992 Feb; 50(2):244-8. PubMed ID: 1613977
[TBL] [Abstract][Full Text] [Related]
31. Glanzmann's thrombasthenia: updated.
Nair S; Ghosh K; Kulkarni B; Shetty S; Mohanty D
Platelets; 2002 Nov; 13(7):387-93. PubMed ID: 12487785
[TBL] [Abstract][Full Text] [Related]
32. Molecular defects in the Bernard-Soulier syndrome: assessment of receptor genes, transcripts and proteins.
Roth GJ
C R Acad Sci III; 1996 Sep; 319(9):819-26. PubMed ID: 8952885
[TBL] [Abstract][Full Text] [Related]
33. Glycoprotein analysis for the diagnostic evaluation of platelet disorders.
Miller JL
Semin Thromb Hemost; 2009 Mar; 35(2):224-32. PubMed ID: 19408195
[TBL] [Abstract][Full Text] [Related]
34. Glanzmann thrombasthenia and Bernard-Soulier syndrome in south Iran.
Afrasiabi A; Artoni A; Karimi M; Peyvandi F; Ashouri E; Mannucci PM
Clin Lab Haematol; 2005 Oct; 27(5):324-7. PubMed ID: 16178914
[TBL] [Abstract][Full Text] [Related]
35. Inherited traits affecting platelet function.
Salles II; Feys HB; Iserbyt BF; De Meyer SF; Vanhoorelbeke K; Deckmyn H
Blood Rev; 2008 May; 22(3):155-72. PubMed ID: 18180086
[TBL] [Abstract][Full Text] [Related]
36. A missense mutation (Tyr88 to Cys) in the platelet membrane glycoprotein Ibbeta gene affects GPIb/IX complex expression--Bernard-Soulier syndrome in the homozygous form and giant platelets in the heterozygous form.
Kurokawa Y; Ishida F; Kamijo T; Kunishima S; Kenny D; Kitano K; Koike K
Thromb Haemost; 2001 Nov; 86(5):1249-56. PubMed ID: 11816714
[TBL] [Abstract][Full Text] [Related]
37. Inherited disorders of platelets and megakaryocytes.
Nurden AT; Pico M; Heilmann E; Jallu V; Hourdillé P
Prog Clin Biol Res; 1990; 356():333-46. PubMed ID: 2217448
[No Abstract] [Full Text] [Related]
38. Novel genetic abnormalities in Bernard-Soulier syndrome in India.
Ali S; Ghosh K; Shetty S
Ann Hematol; 2014 Mar; 93(3):381-4. PubMed ID: 23995613
[TBL] [Abstract][Full Text] [Related]
39. Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.
Kunishima S; Sako M; Yamazaki T; Hamaguchi M; Saito H
Eur J Haematol; 2006 Dec; 77(6):501-12. PubMed ID: 16978236
[TBL] [Abstract][Full Text] [Related]
40. Ultrastructural analysis of megakaryocytes in GPV knockout mice.
Poujol C; Ramakrishnan V; DeGuzman F; Nurden AT; Phillips DR; Nurden P
Thromb Haemost; 2000 Aug; 84(2):312-8. PubMed ID: 10959706
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]